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How to Conduct GCP Inspections / Audits at the Clinical Investigator Site
This course is intended to benefit regulatory good clinical practice (GCP) inspectors and sponsor auditors who audit clinical trials.
- Description
- Curriculum
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Upon completion of this course, you will have an understanding of:
- The procedures involved in planning, conducting and reporting inspections/audits, specifically at clinical investigator sites.
- Some of the general principles described could also be used when conducting inspections at other sites e.g. those of the sponsors and contract research organisations (CRO).
Section 2
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Course details
Duration
1 hour
Lectures
1
Assignments
1